# Looking Beyond Blood Pressure: A Case-Based Approach to Primary Aldosteronism

**Authors:** Pooja Alipuria, Atush Alipuria

PMC · DOI: 10.7759/cureus.102946 · 2026-02-04

## TL;DR

This case study highlights the importance of diagnosing primary aldosteronism in a patient with mild hypertension and subtle symptoms.

## Contribution

The paper presents a case where primary aldosteronism was identified despite non-resistant hypertension and subtle clinical features.

## Key findings

- A patient with mild hypertension and hypokalemia was found to have primary aldosteronism.
- Medical management with a mineralocorticoid receptor antagonist improved blood pressure and resolved proteinuria.
- The case underscores the need for a physiology-based approach to diagnose primary aldosteronism early.

## Abstract

Primary aldosteronism is an underrecognized cause of secondary hypertension, particularly when blood pressure elevation is not resistant and classic features are subtle. We describe a 63-year-old man with long-standing hypertension who presented with generalized weakness and was found to have persistent mild hypokalemia, proteinuria, and concentric left ventricular hypertrophy that appeared disproportionate to the degree of blood pressure elevation. These findings prompted evaluation for primary aldosteronism. Aldosterone-renin ratio testing, performed after correction of hypokalemia and interpreted in the context of ongoing antihypertensive therapy, demonstrated inappropriately elevated aldosterone with suppressed renin. Imaging revealed a unilateral adrenal lesion consistent with an adrenal adenoma. The patient declined surgical intervention and was managed medically with mineralocorticoid receptor antagonist therapy. This resulted in normalization of serum potassium, improved blood pressure control, resolution of proteinuria, and loss of renin suppression on follow-up. This case emphasizes the importance of maintaining a high index of suspicion for primary aldosteronism even when hypertension is not resistant, particularly when mild to moderate blood pressure elevation is accompanied by spontaneous hypokalemia and evidence of renal or cardiac target-organ involvement. An individualized, physiology-based diagnostic approach may facilitate earlier recognition of excess aldosterone and help prevent progression to resistant hypertension and long-term cardiovascular and renal complications.

## Linked entities

- **Diseases:** primary aldosteronism (MONDO:0001422), hypokalemia (MONDO:0003019), proteinuria (MONDO:0003634)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** neuromuscular symptoms (MESH:D020879), pheochromocytoma (MESH:D010673), hypokalemia (MESH:D007008), coronary artery disease (MESH:D003324), adrenal incidentaloma (MESH:C538238), visual distortion (MESH:D006311), cerebrovascular disease (MESH:D002561), renal and cardiac involvement (MESH:C565423), cardiovascular and renal complications (MESH:D002318), endocrine disorders (MESH:D004700), gastrointestinal (MESH:D005767), left ventricular hypertrophy (MESH:D017379), elevated blood pressure (MESH:D006973), ASCVD (MESH:D050197), PA (OMIM:617027), macular hole (MESH:D012167), Proteinuria (MESH:D011507), adrenal lesion (MESH:D000307), adenoma (MESH:D000236), adrenal adenoma (MESH:D018246), diastolic dysfunction (MESH:D018487), obese (MESH:D009765), essential hypertension (MESH:D000075222), prediabetes (MESH:D011236), electrolyte abnormality (MESH:D014883), chronic kidney disease (MESH:D051436), unilateral adrenal lesion (MESH:D000310), -limb weakness (MESH:D018908), diabetes mellitus (MESH:D003920), dyslipidemia (MESH:D050171)
- **Chemicals:** rosuvastatin (MESH:D000068718), amlodipine (MESH:D017311), lipid (MESH:D008055), Spironolactone (MESH:D013148), dexamethasone (MESH:D003907), catecholamine (MESH:D002395), potassium (MESH:D011188), sodium (MESH:D012964), angiotensin receptor blockade (-), cilnidipine (MESH:C065927), Aldosterone (MESH:D000450), telmisartan (MESH:D000077333), atenolol (MESH:D001262), cortisol (MESH:D006854)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12965185/full.md

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Source: https://tomesphere.com/paper/PMC12965185